Patients who received Verteporfin PDT had better visual acuity and contrast sensitivity outcomes at 12 months compared to placebo.
This benefit was especially seen in patients with predominantly classic (>50% of the lesion) CNV.
No statistically significant differences in visual acuity were noted in patients with classic CNV between 0-50% of the lesion area.
|
|
Verteporfin PDT |
Placebo |
Lost at least 15 letters |
Total |
61% |
46% |
|
Classic CNV > 50% of entire lesion |
67% |
39% |
Source Archive